Evidence map›Paper›PMID 39664353›Full record

ArticleIndian journal of orthopaedics2024

Mass Spectrometry Characterization of the Human Ankle and Hindfoot Fracture Microenvironment in Young and Aged Subjects.

John F Dankert, Devan D Mehta, Tori C Rodrick, Evgeny Kanshin, Rown Parola, Beatrix M Ueberheide, Drew R Jones, Kenneth A Egol, Philipp Leucht

Abstract read
In one paragraph

Article in Indian journal of orthopaedics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

John F DankertDepartment of Orthopedic Surgery, NYU Grossman School of Medicine, NYU Langone Orthopedic Hospital, 550 First Avenue, MSB 251, New York, NY 10016 USA.
Devan D MehtaDepartment of Orthopedic Surgery, NYU Grossman School of Medicine, NYU Langone Orthopedic Hospital, 550 First Avenue, MSB 251, New York, NY 10016 USA.
Tori C RodrickMetabolomics Core Resources Laboratory, NYU Langone Health, New York, NY USA.
Evgeny KanshinProteomics Laboratory, Division of Advanced Research Technologies, New York University Grossman School of Medicine, New York, NY USA.
Rown ParolaDepartment of Orthopedic Surgery, NYU Grossman School of Medicine, NYU Langone Orthopedic Hospital, 550 First Avenue, MSB 251, New York, NY 10016 USA.
Beatrix M UeberheideProteomics Laboratory, Division of Advanced Research Technologies, New York University Grossman School of Medicine, New York, NY USA.
Drew R JonesMetabolomics Core Resources Laboratory, NYU Langone Health, New York, NY USA.
Kenneth A EgolDepartment of Orthopedic Surgery, NYU Grossman School of Medicine, NYU Langone Orthopedic Hospital, 550 First Avenue, MSB 251, New York, NY 10016 USA.
Philipp LeuchtDepartment of Orthopedic Surgery, NYU Grossman School of Medicine, NYU Langone Orthopedic Hospital, 550 First Avenue, MSB 251, New York, NY 10016 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bone regeneration following a fracture is dependent on multiple factors including skeletal stem cells (SSCs). Recruitment, proliferation, and differentiation of the SSCs is guided by the proteins and metabolites found within the fracture microenvironment. Understanding how intrinsic factors affect the fracture microenvironment has been a topic of ongoing investigation. This study sought to determine whether the levels of select proteins and metabolites within the fracture hematoma would be differentially expressed depending on the age of the patient. We hypothesized that a distinct set of proteins and metabolites found within the fracture hematoma microenvironment would be present at varying levels depending on patient age. Methods: The research study was reviewed and approved by an Institutional Review Board. Hematomas were collected from subjects aged 18 years old or older undergoing surgical intervention for a fracture. Hematoma samples were selected from the biorepository and assigned to one of two fracture groups including young ankle/hindfoot and aged ankle/hindfoot. Protein and metabolite levels within each hematoma were analyzed by liquid chromatography-mass spectrometry. Results: A total of seven hematomas were included in each the young ankle/hindfoot and aged ankle/hindfoot groups. From the global metabolomic analysis, creatine, 2-methylindoline, and acetyl-L-carnitine were identified as being differentially expressed between both groups. An untargeted metabolomic analysis of the two groups identified significant differences in the levels of an additional 66 metabolites. Proteomic analysis identified 34 proteins that were expressed at significantly different levels. Conclusions: The level of metabolites and proteins found within the local fracture environment vary by patient age. Future investigations will focus on identifying a role for these proteins and metabolites in bone homeostasis and fracture healing. Level of Evidence: N/A, basic science investigation. Supplementary Information: The online version contains supplementary material available at 10.1007/s43465-024-01284-3.

Indexed as

BiologicsFractureMass spectrometryMicroenvironmentNon-union

Identifiers

PMID39664353
PMCPMC11628468

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.